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Plos One|February 5, 2026
Prognostic role of interim F-18 fluorodeoxyglucose positron emission tomography-computed tomography during chemoradiation therapy in patients with hypopharyngeal squamous cell carcinomaTakamitsu Mase, Yutaka Toyomasu, Hajime Ishinaga, et al.Stem Cell Reports|March 20, 2026
Deuterosomal cells are the responsible lineage for multiciliogenesis in human airway differentiationHaruka Yamaki, Satoshi Konishi, Koji Tamai, et al.Sustainability Science|November 4, 2020
Beyond 2020: converging crises demand integrated responses: Statement by the RACC International Advisory Committee following the RACC-12 International ForumJim Falk, Rita Colwell, Adel El-Beltagy, et al.Molecular Genetics & Genomic Medicine|January 22, 2020
Copy number variation in DRC1 is the major cause of primary ciliary dyskinesia in the Japanese populationKazuhiko Takeuchi, Yifei Xu, Masako Kitano, et al.Dermatopathology (Basel, Switzerland)|August 23, 2022
A Case of IgG and IgA Anti-Laminin-332 Antibody-Positive Mucous Membrane Pemphigoid with IgG and IgA Anti-Envoplakin and Anti-Periplakin AntibodiesYoshiaki Matsushima, Masako Kitano, Daisuke Hayashi, et al.Respiratory Investigation|February 16, 2021
Multifaceted analysis of Japanese cases of primary ciliary dyskinesia: Value of immunofluorescence for ciliary protein detection in patients with DNAH5 and DNAH11 mutationsAtsushi Kurokawa, Mitsuko Kondo, Mami Orimo, et al.Respirology Case Reports|May 18, 2026
Immunostaining and Ciliary Movement Analysis in Primary Ciliary Dyskinesia With a Homozygous Deletion Involving Exons 1-4 of DRC1: A Case ReportAtsushi Kurokawa, Mitsuko Kondo, Mayoko Tsuji, et al.European Journal of Pharmacology|February 27, 2004
Effects of a 20-HETE antagonist and agonists on cerebral vascular toneMing Yu, Liana Cambj-Sapunar, Franz Kehl, et al.Auris, Nasus, Larynx|August 29, 2021
Analysis of the clinical features of Japanese patients with primary ciliary dyskinesiaKazuki Chiyonobu, Yifei Xu, Guofei Feng, et al.Case Reports in Genetics|August 19, 2024
Two Pediatric Cases of Primary Ciliary Dyskinesia Caused by Loss-of-Function Variants in Oral-Facial-Digital Syndrome Gene, OFD1Yifei Xu, Yuki Tsurinaga, Tsubasa Matsumoto, et al.Pageof 17